FDA applicant

Medicon EG

Tuttlingen, DE17 decisions1995–20170 recalls

FDA records 17 decisions for Medicon EG (Tuttlingen, DE) from 1995 to 2017: 17 510(k) clearances. Most are in product codes JEY (Plate, Bone) and DZE (Implant, Endosseous, Root-Form). Its devices cite 24 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Medicon EG’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2007high 2 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medicon EG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medicon EG’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Medicon”

FDA records each applicant name separately; these may or may not be the same firm.

Medicon, Inc. 15 Medicon Instruments, Inc. 6 Medicon Hellas S.A 3

Medicon EG

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medicon”